EP2401228A1

EP2401228A1 - Production of iron orthophosphate

Info

Publication number: EP2401228A1
Application number: EP10707487A
Authority: EP
Inventors: Gunnar BÜHLER; Kilian Schwarz
Original assignee: Chemische Fabrik Budenhiem KG
Current assignee: Chemische Fabrik Budenhiem KG
Priority date: 2009-02-26
Filing date: 2010-02-19
Publication date: 2012-01-04
Anticipated expiration: 2030-02-19
Also published as: IL214044A; DE102009001204A1; KR20110139190A; MY151233A; SG172357A1; HK1164262A1; JP5748146B2; WO2010097341A1; CN102333725B; AU2010217661A1; CA2747646A1; AU2010217661B2; MX2011008607A; IL214044A0; EP2401228B1; RU2011139174A; ES2599972T3; KR101690141B1; US8574518B2; BRPI1009769A2

Abstract

The invention relates to a method for producing iron(lll)orthophosphate of general formula FePO4 x nH2O (n = 2,5), in which a) an aqueous solution containing Fe2+-ions is produced, in which oxidized iron (ll)-, iron (lll) or mixed iron (ll,lll) compounds selected from hydroxides, oxides, oxide hydroxides, oxide hydrates, carbonates and hydroxide carbonates, together with elementary iron are introduced into an aqueous medium containing a phosphorous acid and Fe2+-ions are introduced into a solution and Fe3+ are transformed into Fe2+ with elementary Fe (in a comproportionation reaction), b) solids are separated from the aqueous phosphoric acid Fe2+ solution, c) an oxidation agent is added to the aqueous phosphoric acid Fe2+solution, in order to oxidate the iron (ll) in the solution, and iron (lll)orthophosphate of general formula FePO4 x nH2O precipitates.

Description

Production of iron orthophosphate

The present invention relates to a process for the preparation of iron (III) orthophosphate with particularly high purity, an iron (III) orthophosphate prepared by the process and its use for the production of LiFePO ₄ cathode material for Li-ion accumulators, as dietary supplement for mineral enrichment as well as molluscicide.

Iron phosphates are used in many areas, for. As a dietary supplement or as a food additive for mineral enrichment, as an active ingredient in molluscicides, in the ceramics industry or as a raw material for the production of LiFePO ₄ cathode material for Li ion batteries. Each field of application makes individual demands on the iron phosphate, wherein in some applications, in particular, the chemical purity is of particular importance. In many cases, the morphology or the particle fineness of the iron phosphate has a critical importance for the success of the application, eg. When considering bioavailability for organisms.

Rechargeable Li-ion batteries are widely used energy storage, especially in the field of mobile electronics, as the Li-ion battery is characterized by a high energy density and can deliver a high rated voltage of 3.7 volts, so that the Li-ion battery at comparable performance is significantly smaller and lighter than conventional accumulators. As cathode materials, spinels such as LiCoθ ₂ , LiNiO ₂ , LiNi _1-x Co _x θ ₂ and LiMn _n O _{4 have been} established. To increase the safety of Li-ion batteries, especially in terms of thermal overload during operation, LiFePO ₄ was developed as a cathode material. This material features better performance, higher specific capacity and high thermal stability during operation.

High purity requirements are placed on the cathode material of a rechargeable battery since any contamination that may undergo undesirable redox reactions during operation (charging or discharging) adversely affects the performance of the rechargeable battery. The type and concentration of possible contaminations depends essentially on the quality of the raw materials used to produce the cathode material. In the manufacturing process of the cathode material, measures can be taken for the subsequent reduction of impurities, but this is generally associated with an increase in the production costs. is bound. It is therefore desirable to use as pure starting materials or raw materials for the production of the cathode material.

A starting material for the production of LiFePO ₄ for lithium-ion accumulators is ice northophosphate, the purity and structure or morphology of which significantly influences the quality of the cathode material produced therefrom.

Known processes for the preparation of iron (III) orthophosphate use FeSO ₄ and FeCb as starting materials or raw materials, but also organometallic precursor compounds, such as FeC ₂ O ₂ (Gmelin's Handbook of Inorganic Chemistry, Part B Iron, pages 773 et seq., US Pat. C. Delacourt et al., Chem. Mater., 2003, 15, 5051-5058; Zhicong Shi et al., Electrochemical and Solid State Letters 2005, 8, A396-A399). The phosphorus or phosphate component is introduced in these starting materials via a phosphate salt or phosphoric acid. Additions of HCl, NaOH, NH ₃ , NaCIO ₃ or surfactants are always necessary in the processes described in order to control the chemical-physical properties of the products obtained. As a result, the materials thus produced always contain impurities of anions, such as chloride or sulfate, cations, such as sodium or ammonium, or organic components. On an industrial scale, these impurities can only be removed, if at all, by the most expensive and costly cleaning processes.

Further cationic contamination, such. B. transition metals that were originally contained in the raw materials used such as FeSO ₄ or FeCl ₃ , can not be easily separated or washed out in general, since they also form sparingly soluble phosphate salts in general and crystallize together with the desired iron phosphate.

WO 02/30815 describes a process for the preparation of LiFePO ₄ from iron phosphate and lithium, wherein an iron oxide is dissolved in 85% phosphoric acid with heating to produce the iron phosphate. The solution is then diluted until the solubility limit of FePO _{4 is} reached and the material crystallizes. By fractional dilution in this case unwanted metal phosphates are to be separated, which have a smaller solubility product than FePO. ₄ This method has the disadvantage that it requires a very high energy input and a lot of water is needed to precipitate the product. In this process, a soluble complex of iron is formed, which is stable for weeks and crystallizes only slowly. This significantly reduces the economic yield of the product. By boiling the solution for several days, the yield can be increased, which, however, requires a very large amount of energy. In addition, the process involves a large amount of dilute Phosphoric acid, which can be re-used in the process only after concentration. The method is therefore not interesting from an economic as well as ecological point of view.

The prior art processes for producing iron phosphates have further disadvantages when the resulting iron phosphate product is to be used to produce LiFePO ₄ for Li-ion batteries. Important considerations for the suitability of the material are the morphology and the particle size distribution of the iron phosphates. By the methods of precipitation of iron phosphate according to the prior art, spherical crystals of different size are generally obtained. However, these have a small surface area compared to other crystal morphologies. For use as a cathode material in Li-ion batteries, iron phosphate having a large crystal surface is advantageous for ensuring penetration of lithium ions in a large number and at high speed. Moreover, it is advantageous to obtain crystals of small size in order to reduce the diffusion distances and times of the lithium ions. Furthermore, a high bulk density and compressibility of the material is desired in order to realize a high energy storage density in the produced cathode material.

Some of the aforementioned disadvantages and problems of the prior art are overcome by an iron orthophosphate and a process for its preparation according to the copending German patent application DE 102007049757. In the process, oxidic iron (II), iron (III) or mixed iron (II, III) compounds are reacted with phosphoric acid at a concentration in the range of 5% to 50% and optionally present iron (II) after the reaction. converted by the addition of an oxidizing agent in iron (IM) and solid iron (III) orthophosphate separated from the reaction mixture. Iron (III) present in the starting material is precipitated directly as iron (III) orthophosphate by the addition of the phosphoric acid. However, the method has the disadvantage that in the course of the reaction always partially the raw materials and the product are present as solids side by side. A separation of impurities, either as a solution or as solids, is not possible. In order to achieve a high chemical purity of the product, it is therefore dependent on the quality and purity of the raw materials and set.

The object of the present invention was therefore to provide an iron (III) orthophosphate and a process for its preparation in which the known disadvantages of the prior art are overcome and in comparison with known production processes iron (III) orthophosphate in a simpler manner high purity is available. The object of the present invention is achieved by a process for the preparation of iron (III) orthophosphate of the general formula FePO ₄ .xNH ₂ O (n <2.5), in which a) a Fe ²⁺ -lene-containing aqueous Solution is prepared by oxidic iron (II) -, iron (III) - or mixed iron (II, III) compounds selected from hydroxides, oxides, oxide hydroxides, oxide hydrates, carbonates and hydroxide, together with elemental iron in a phosphoric acid containing introducing aqueous medium and solubilizing Fe ²⁺ ions and reacting Fe ³⁺ with elemental Fe (in a comproportionation reaction) to form Fe ²⁺ ; b) separating solids from the aqueous phosphoric Fe ²⁺ solution; phosphoric acid aqueous Fe ²⁺ solution adds an oxidizing agent to oxidize iron (II) in the solution, and iron (III) orthophosphate of the general formula FePO ₄ x nH ₂ O precipitates.

In the process according to the invention, the starting materials (oxidic iron raw material, elemental iron) in powder form, preferably in particle sizes D50 in the range of 0.01 .mu.m to 300 .mu.m, used and directly with the phosphoric acid-containing aqueous medium, preferably with dilute phosphoric acid, mixed and implemented. Alternatively, the starting materials or some of the starting materials can first be freshly produced via precipitation and any subsequent annealing and then further processed as a filter cake. This results in a slurry colored by the solid content of the raw material (black to brown to red).

As used herein, aqueous solvent includes embodiments containing only water as the liquid medium, as well as those embodiments in which the liquid medium is predominantly water, but also portions of water-miscible organic and / or ionic solvents or liquids. It is known that such solvent additives can have an influence on the crystal growth and thus on the resulting morphology of the product.

In the aqueous medium containing phosphoric acid, a redox reaction occurs between Fe ³⁺ from the oxidic iron raw material and the elemental iron, soluble Fe ^{2+ being} formed in a proportioning ratio according to the following reaction equation (I).

(I) 2 Fe ³⁺ + Fe - »3 Fe 2+ The reaction mixture is heated to about 2 to 25 ° C depending on the raw material, if the resulting heat of reaction is not dissipated, which is not necessary in principle. After the reaction has subsided, the mixture is heated with stirring to higher temperatures, preferably below 65 ° C, wherein the introduced solids more or less completely react depending on the composition and purity to form a typically green-colored Fe ²⁺ solution. After about 50 to 120 minutes, this process step is completed. The duration depends among other things on the raw materials and concentrations used.

Depending on the purity of the solids used a more or less pronounced turbidity remains in the solution, which is caused by compounds which are insoluble under the reaction conditions. This remaining solids content can be removed by simple filtration, sedimentation, centrifugation or other suitable means. The doses of these solids vary depending on the choice of starting materials used in the process, acid concentration and reaction temperature.

In order to remove further impurities or undesirable substances and compounds from the solution, precipitation reagents defined with advantage can be added to the solution. So z. B. the calcium content in the solution can be reduced by adding small amounts of sulfuric acid with precipitation of calcium sulfate. Furthermore, an additional electrolytic precipitation or deposition of unwanted metal ions from the solution can advantageously also be carried out before iron (III) is produced in the iron (II) solution by oxidation and the iron (III) orthophosphate is precipitated.

An advantage of the process according to the invention is that a homogeneous phosphoric acid aqueous iron (II) solution is prepared as an intermediate, from which all impurities present as solids or can be converted into solids or precipitated by precipitation additives can be separated off by simple means before being dissolved in the purified ferrous solution produced as an intermediate produces the iron (III) orthophosphate by oxidation and precipitates again as a solid. The solid iron (III) orthophosphate is therefore not present in the aqueous solution at the same time as other insoluble starting compounds originally used, as is the case, for example, in the process according to the copending German patent application DE 102007049757. Compared with other processes, the process according to the invention permits the preparation of iron (III) orthophosphate with high purity, without it being necessary subsequently to carry out particularly expensive purification processes. In one embodiment of the inventive method, the reaction of the oxide iron compounds together with elemental iron containing phosphoric acid in an aqueous medium is carried out at a temperature ranging from 15 ° C to 90 ⁰ C, preferably in the range of 20 ⁰ C to 75 ° C, more preferably in the range of 25 ° C to 65 ° C by. If the temperature is too low, the reaction rate is slow and possibly uneconomical. If the temperature is too high, premature precipitation of iron (III) orthophosphate may partly occur due to possible solid-state reaction of the solid starting materials contained in the suspension. Furthermore, by too high a temperature, the course of side reactions, as described below, is promoted.

Conveniently, the reaction of the oxidic iron compounds together with elemental iron in aqueous medium containing phosphoric acid is carried out with thorough mixing, preferably with stirring. For this purpose, all known in the art mixers and stirrers, which are suitable for such a purpose can be used. It is also advantageous to use jet mixers, homogenizers, flow reaction cells, etc. for mixing and / or moving the reaction mixture.

In a further embodiment of the process according to the invention, the reaction of the oxidic iron compounds together with elemental iron in aqueous medium containing phosphoric acid is carried out for a period of from 1 minute to 120 minutes, preferably from 5 minutes to 60 minutes, more preferably from 20 minutes to 40 minutes , The reaction of the iron compounds together with elemental iron in phosphoric acid-containing aqueous medium can of course be stopped at any time by separating the solids from the aqueous solution, which may have a yield loss in incomplete reaction.

In the method according to the invention, the concentration of phosphoric acid in the aqueous medium is suitably 5% to 85%, preferably 10% to 40%, more preferably 15% to 30%, based on the weight of the aqueous solution. Low phosphoric acid concentrations are economically advantageous, the reaction can proceed very slowly at too low a concentration, which may also be undesirable from an economic point of view. At high phosphoric acid concentrations, such as over 35%, depending on the fineness of the oxidic iron compounds used, their clumping can occur, which considerably increases the duration of the above-described comproportionation reaction between Fe ³⁺ and elemental iron. It also became an influence of phosphoric acid concentration observed on the fineness of the final product. Thus, a lower concentration of phosphoric acid tends to result in a finer final product having a mean particle size D50 <35 microns, whereas a higher phosphoric acid concentration tends to promote the production of a coarser end product having an average particle size D50> 35 microns. The phosphoric acid concentration can be adjusted for the precipitation step after the co-proportioning reaction between Fe ³⁺ and elemental iron by adding concentrated phosphoric acid or water, or removing contained water by evaporation. This makes it possible to control the fineness of the final product iron (III) orthophosphate independently of the amounts of raw material used to produce the Fe ²⁺ solution.

In a side reaction between the elemental iron and the phosphoric acid, hydrogen gas is produced according to the following reaction equation (II), which must be deliberately removed for safety reasons.

(II) Fe + H ₃ PO ₄ Fe ²⁺ + HPO ₄ ^{2 "} + H ₂

This side reaction can not be suppressed, so that a stoichiometric excess of elemental iron must always be used in comparison with the amount required for the reaction of Fe ³⁺ in the oxidic iron raw material in accordance with reaction equation (I) given above. The exact amount of this excess largely depends on the reaction conditions, such as the fineness or surface activity of the solids used, the temperature and the acid concentration. An excess of a few percent of the stoichiometric amount has proven sufficient in many cases. At temperatures above 40 ⁰ C, an increase in the rate of side reaction was observed. Above 70 ° C, a simultaneous precipitation of iron orthophosphate can be used so that no homogeneous Fe ²⁺ solution is obtained. If it comes to the above-mentioned clumping of the oxidic iron component, the elemental iron reacts largely on the side reaction. The corresponding stoichiometries are therefore to be adapted to the particular reaction conditions chosen and to the reactivity of the raw materials used.

After dissolving the iron (II) from the oxidic starting material and reacting the iron (III) and the elemental iron by Komproportionierung to iron (II) after the removal of any impurities described above, the heating of the reaction stops or the temperature on expediently limited to about 85 to 100 ⁰ C and added oxidizing agent until essentially the entire proportion of iron (II) was oxidized to iron (III) and no more iron (II) can be detected or a given Iron (II) concentration is below. Under these conditions, iron (III) orthophosphate precipitates as a off-white to slightly pink colored solid. The aforesaid temperature range of about 85 to 100 ^° C. is preferred according to the invention for the oxidation and precipitation stage, but other temperature ranges are not excluded. The product may be separated by filtration or other common procedures as a solid. Drying at different drying intensities makes it possible to obtain various products of the general formula FePO ₄ .xH ₂ O (n <2.5).

By adjusting the acid concentration already at the beginning of the dissolution process, or later just before or during the oxidation process, the morphology of the product can be controlled. A high bulk density product is obtained by performing the precipitation at an acid concentration of 23-25%. At higher and lower concentrations, products with low bulk densities are obtained.

In a preferred embodiment of the process according to the invention, the oxidizing agent which is added to oxidise iron (II) in the solution is an aqueous solution of hydrogen peroxide (H ₂ O ₂ ). The hydrogen peroxide solution preferably has a concentration of 15 to 50 wt .-%, particularly preferably 30 to 40 wt .-%.

In alternative embodiments of the process of the invention, the oxidizing agent added to oxidize iron (II) in the solution is a gaseous medium selected from air, pure oxygen or ozone, which is injected into the aqueous solution.

The oxidation by adding a suitable oxidizing agent is preferably carried out immediately after the separation of the solids from the phosphoric acid aqueous Fe ²⁺ solution. In the oxidation reaction, the temperature of the reaction mixture may be maintained at or near the temperature previously set for the reaction of the iron compounds. Preferably, a temperature range of about 85 to 100 ⁰ C. Alternatively the oxidation may be carried out onsreaktion including after cooling the solution to room temperature or, whereby the precipitation of the iron formed (III) orthophosphate but is not favored. Both the oxidation reaction and the precipitation of the iron (III) orthophosphate formed generally proceed more readily and more rapidly at elevated temperature, which is why it is preferred to carry out this step at a moderately elevated temperature. The oxidation reaction is carried out until no or substantially no more iron (II) is detectable in the reaction mixture. For the detection of iron (II) in the aqueous solution, rapid tests (eg test strips or test strips) known to the person skilled in the art are available whose accuracy is sufficient for the purposes of the present invention. The separation of the iron (III) orthophosphate from the aqueous solution is preferably carried out by filtration, sedimentation, centrifuging or combinations of the aforementioned separation methods. Conveniently, the separated from the reaction mixture iron (III) orthophosphate is then dried at elevated temperature and / or under reduced pressure. Alternatively, the iron (III) orthophosphate after separation can also advantageously be further processed in moist form as filter cake or dispersion with solids contents of 1 to 90% by weight, depending on the possible or desired efficiency of the dewatering step.

The process according to the invention for the preparation of iron (III) orthophosphate also has some ecological and economic advantages over other known processes in addition to the achievable high purity of the end product. The mother liquor remaining after the separation of iron (III) orthophosphate contains substantially no contaminating reaction products, such as, for example, sulfates or chlorides, which are left behind in the known prior art processes using iron sulfate or iron chloride as the starting material. Mother liquor from the process according to the present invention can therefore be adjusted again to the desired concentration by adding concentrated phosphoric acid and is thus completely traceable back into the process. This saves costs and avoids unwanted waste.

The present invention also includes iron (III) orthophosphate prepared according to the process of the invention described herein.

The iron (III) orthophosphate according to the invention is not only simpler and less expensive to produce than the prior art, it also differs structurally and in terms of its composition or impurities from iron (III) orthophosphate, according to known art Method was made from the prior art. Among others, the iron (II), iron (III) and mixed iron (II, III) compounds used as starting materials also contribute to this, chosen from hydroxides, oxides, oxide hydroxides, hydrated oxides, carbonates and hydroxide carbonates. In contrast to the present invention, known processes for the preparation of iron (III) orthophosphate according to the prior art employ, inter alia, iron sulphate or sulphate-containing raw materials and / or nitrate-containing raw materials and control the course of the pH of the reaction. tion with caustic soda. The resulting iron phosphates therefore contain high residues of sulfur, predominantly in the form of sulfate, nitrate and sodium.

Too high a content of sulfur, usually present as sulphate, and too high a content of nitrate affect the quality of a LiFePO ₄ produced from the iron (III) orthophosphate.

Cathode material for Li-ion batteries, since these anions contain undesirable redox

Reacting. In one embodiment of the present invention, therefore, the iron (III) orthophosphate has a sulfur content of <300 ppm, preferably <200 ppm, more preferably <100 ppm. In a further embodiment of the present invention, the iron (III) orthophosphate or a nitrate content of <300 ppm, preferably

<200 ppm, more preferably <100 ppm.

Sodium and potassium cations also affect the quality of an LiFePO ₄ cathode material made from the iron (III) orthophosphate since they can occupy lithium sites. In a further embodiment of the invention, the iron (III) orthophosphate therefore has a content of sodium and potassium of <300 ppm, preferably <200 ppm, particularly preferably <100 ppm.

Excessive contamination of metals and transition metals also affect the quality of a LiFePO ₄ cathode material made from the iron (III) orthophosphate. In a further embodiment of the invention, the iron (III) orthophosphate therefore has a content of metals and transition metals, with the exception of iron, of in each case <300 ppm, preferably

<200 ppm, more preferably <100 ppm.

The properties of the product according to the invention, namely the iron (III) orthophosphate according to the invention, are substantially influenced by its preparation process and the starting materials used for its preparation and differ from iron (III) orthophosphate according to the prior art.

Iron (III) orthophosphates prepared by well-known methods from iron sulfate or iron chloride also have differences in crystal structure. X-ray structural investigations have shown that iron (III) orthophosphates prepared from iron sulphate or iron chloride according to the prior art are present predominantly in the metastrite I structure with small amounts of strengite and metastrengite II (phosphosiderite). On the other hand, X-ray structural studies on iron (III) prepared according to the invention revealed orthophosphates found that these are predominantly present in the metastatic it Il structure (phosphosiderite) with very low or undetectable levels of strengite and metastases.

In one embodiment of the iron (III) orthophosphate according to the invention, therefore,> 80% by weight, preferably> 90% by weight, particularly preferably> 95% by weight, of the iron (III) orthophosphate in the M etastreng II. (Phosphosiderite) crystal structure before.

The occurrence of the three previously described allotropic forms of iron (III) orthophosphate (Metastrengite I, M etastreng it II and Strengit) is described in the literature as well as the difficulty of producing a phase-pure system (C. Delacourt et al., Chem. Mater., 2003, 15, 5051-5058). Contrary to the reservations expressed in the literature, the inventors have now found that with the method described herein, the iron (III) phosphate in the metastrengite II structure is also in a remarkably pure form in a pH range determined solely by the phosphoric acid leaves.

The iron (III) orthophosphate according to the invention preferably has a platelet-shaped morphology with metastrengite II structure. This structure allows a much denser packing of the crystallites and particles with a smaller exclusion volume compared to spherical particles. With the iron (III) orthophosphate according to the invention, high bulk densities and tamped densities can therefore be realized, which is particularly advantageous for use in LiFePCU cathode materials. A small thickness of the platelets ensures, for example, a high reaction rate in the production of LiFePO ₄ and a higher performance of the finished cathode material, since the diffusion distances and diffusion times of Li ions compared to conventional material can be significantly reduced. In addition, layered aggregates / agglomerates of this material can easily be converted into dispersions of the primary particles by conventional methods under the action of shearing forces (Turrax, agitator ball mill, ultrasound, etc.).

In one embodiment of the invention, the iron (III) orthophosphate is in the form of platelet-shaped crystals. Preferably, these crystals have a small thickness in the range of less than 1000 nm, preferably <500 nm, more preferably <300 nm, most preferably <100 nm. The dimensions of the platelet-shaped crystals in the two dimensions perpendicular to the thickness are preferably in the range of 200 to 2000 nm, more preferably 300 to 900 nm, most preferably 400 to 800 nm. Furthermore, in a preferred embodiment, the iron (III) orthophosphate according to the invention has a bulk density of> 400 g / l, preferably> 700 g / l, particularly preferably> 1000 g / l. In a further embodiment, the iron (III) orthophosphate according to the invention has a tapped density of> 600 g / l, preferably> 750 g / l, more preferably> 1100 g / l.

The iron (III) orthophosphate according to the invention thus exhibits a very fine primary particle size and, at the same time, a very high attainable bulk density or a high tamped density. This was surprising compared to the prior art. Iron (III) orthophosphates, which are prepared by generally known methods from iron sulfate or iron chloride, usually have a primary particle size of> 1 .mu.m, which also high bulk densities of> 1000 g / l can be realized. If corresponding iron (III) orthophosphates with smaller primary particle sizes in the sub-micron range are prepared according to these known processes from iron sulfate or iron chloride, then only low bulk densities of up to 400 g / l can be achieved. The reasons for this probably lie in the particle morphology influenced by the crystal structure and the particle size distribution. The morphology of iron (III) phosphates, which are prepared by generally known methods from iron sulfate or iron chloride, consists predominantly of spherical particles, whereas the iron (III) orthophosphate according to the invention has the previously described morphology with a high proportion of angular, platy - has chenförmigen crystals.

The present invention also encompasses the use of the iron (III) orthophosphate according to the invention for the production of Li FePCU cathode material for Li-ion accumulators. The preparation of such a cathode material using iron (III) orthophosphate is known per se to a person skilled in the art, but here the iron (III) orthophosphate according to the invention offers the particular advantages described above.

Further, the present invention encompasses LiFePCU cathode material for Li-ion accumulators made using iron (III) orthophosphate as described and claimed herein, and Li-ion accumulators comprising a LiFePCU cathode material of the aforementioned kind ,

In a further aspect, the invention also encompasses the use of the iron (III) orthophosphate according to the invention as a food supplement and for the mineral enrichment of foods, since it is suitable for food and has a very high bioavailability for the organism. It is particularly advantageous here to use the iron (III) orthophosphate according to the invention in the form of aqueous dispersions. In a further aspect, the invention also encompasses the use of the iron (III) orthophosphate according to the invention as a molluscicide, for example in the control of snails. Iron (III) orthophosphate is known per se for its molluscicidal activity. It leads to a slime of the animals. The iron (III) orthophosphate according to the invention is particularly effective because of its structurally high bioavailability compared to conventionally prepared iron (III) phosphate, so that less substance is needed to achieve the same effect. The iron (III) orthophosphate according to the invention in the form of aqueous dispersions is used with particular advantage here.

Further advantages, features and embodiments of the present invention will become apparent from the following examples which illustrate but are not intended to limit the present invention.

Examples

example 1

A diluted phosphoric acid (18Gew .-%; density = 1, 146 g / ml at 20 ⁰ C) At room temperature (RT; 20 ⁰ C) introduced and mixed with 20 g of iron oxide (magnetite, Fe _S U ₄₎ was added. The batch is homogenized at 10,000 rpm for 10 min with a dispersing rod. Subsequently, the resulting suspension is mixed with stirring with 7 g of iron powder.

It uses an exothermic reaction. The temperature rises from about 20 ⁰ C to about 40 ⁰ C within 20 min. The suspension changes its color from black to green-brown over this period, and the starting material goes into solution. Small bubbles in the suspension indicate that gas evolution (H ₂ ) occurs. With a bubble counter, the amount of gas produced was quantified. After the dissolution process is complete, the solution is filtered to separate solids from the solution. Subsequently, the solution is heated to 80 ⁰ C and treated with about 55 ml of H ₂ O ₂ (35 wt .-%) to the Fe in the solution ²⁺ ions to be oxidized to Fe ³⁺ ions. As a decomposition product of H ₂ O ₂ . arises oxygen. A rapid test for Fe ²⁺ ions (test strips from Merck) is used to check whether the oxidation reaction is complete. If appropriate, H ₂ O _{2 is} replenished. Subsequently, the now pink-colored solution is kept at about 85 ° C and precipitated iron (III) orthophosphate. The failure takes about 30 minutes. The final product is light pink and is filtered off with suction through a frit and washed with 400 ml of water. The finer the material, the longer the suction process can take. The product is then dried in a drying oven for 3 h at 80 ⁰ C. The yield is at least 90%. The final product is a fine iron (11) orthophosphate.

Example 2

As Example 1, but a slightly higher concentrated phosphoric acid is presented (25 wt .-%, density = 1.208 g / ml at 20 ⁰ C), and after the oxidation reaction, the iron (III) orthophosphate is precipitated at 100 ⁰ C. The yield is over 90%. The final product is a crude iron (III) orthophosphate compared to Example 1.

Example 3

20 g of Fe 3 O ₄ are initially charged in 125 g of H ₂ O and pretreated with an Ultraturrax at 10,000 rpm for 30 min. Subsequently, 125 g of 75% phosphoric acid, a further 125 g of H ₂ O and 7 g of Fe are added at RT. The density of dilute phosphoric acid in the batch is 1.146 g / ml at 20 ^° C. There is slight gas evolution over the entire reaction period stops. Within 7 minutes, the temperature rises to 42 ° C and the color of the suspension changes to brown. After 9 minutes no further increase in temperature is detected and therefore the reaction mixture is heated in an oil bath (T = 120 ° C). After 70 minutes there is a green solution which has a very low turbidity. Further gas development is no longer observed. The turbidity is removed by filtration and the filtrate with 40 ml of H ₂ θ ₂ -Lsg (35% by weight) at 80 ⁰ C added. It turns a color change over intense red to light pink, the product precipitating as a fine solid with light pink color. The yield is 99.8% (71.7 g).

Example 4 20 g of Fe 3+ ₄ , 7 g of Fe, 250 g of H ₂ O and 125 g of 75% strength phosphoric acid are combined at RT. The density of dilute phosphoric acid in the batch is 1.146 g / ml at 20 ^° C. There is slight gas evolution which persists throughout the reaction period. Within 20 minutes, the temperature rises to 38 ° C and the color of the suspension changes to brown. After 30 minutes no further increase in temperature is detected and therefore the reaction mixture is heated in an oil bath (T = 120 ° C). After 90 minutes there is a green solution which has a very low turbidity. Further gas evolution is no longer observed. The turbidity is removed by filtration and the filtrate is mixed with 40 ml of H ₂ O ₂ -LSg (35 wt .-%) at 85 ° C. It turns a color change over intense red to light pink, the product precipitating as a fine solid with light pink color. The yield is 83.5% (60.0 g).

Example 5

20 g FeßCU, 7g Fe, 250g H ₂ O and 204g 75% phosphoric acid are combined at RT. The density of dilute phosphoric acid in the batch is 1.32 g / ml at 20 ^° C. There is slight gas evolution which persists throughout the reaction period. Within 10 minutes the temperature rises to 53 ° C and the color of the suspension changes to brown. It is immediately cooled with an ice bath at 50 ⁰ C. After a further 40 min at 50 ⁰ C, a green solution is present, which has a very low turbidity. Further gas evolution is no longer observed. The turbidity is removed by filtration and the filtrate with 40 ml H ₂ O ₂ solution. (35 wt .-%) at 85 ° C added. It turns a color change over intense red to light pink, the product precipitates as a coarse solid with light pink color. The yield is 85.8% (61, 6g). Example 6

10 g Fe ₂ θ3, 3.2 g of Fe, 21 1g H ₂ O and 93g 75% phosphoric acid are added together at 50 ⁰ C. The density of the dilute phosphoric acid in the batch is 1.134 g / ml at 20 ^° C. There is slight gas evolution which persists throughout the reaction period. After 157 min at 50 ⁰ C, a green solution is present, which has a very low turbidity. Further gas evolution is no longer observed. The turbidity is removed by filtration and the filtrate with 20 ml H ₂ O ₂ -L-Sg. (35 wt .-%) at 85 ° C added. It turns a color change over intense red to light pink, the product precipitating as a fine solid with light pink color. The yield is 30.2 g.

Example 7

10 g of Fe ₂ O 3, 11 g of Fe, 379 g of H ₂ O and 168 g of 75% strength phosphoric acid are combined at RT. The density of the dilute phosphoric acid in the batch is 1.134 g / ml at 20 ^° C. There is slight gas evolution which persists throughout the reaction period. It is heated to 63 ° C and after 120 min a green solution obtained, which has a very low turbidity. Further gas evolution is no longer observed. The turbidity is removed by filtration and the filtrate with 30 ml H ₂ O ₂ solution. (35 wt .-%) at 85 ° C added. It turns a color change over intense red to light pink, the product precipitating as a fine solid with light pink color. The yield is 58g.

figure description

FIG. 1 a shows a scanning electron micrograph of an iron (III) orthophosphate having a metastrengite I crystal structure prepared from a known process according to the prior art from Fe (II) SO ₄ with phosphoric acid.

FIG. 1b shows an XRD spectrum in the angular range of 5 ° to 70 ° 2 theta of the iron (III) orthophosphate from FIG. 1a.

FIG. 2 a shows a scanning electron micrograph of iron (III) orthophosphate according to the invention, prepared according to Example 1, which is present predominantly in the metasthere I 1 crystal structure.

FIG. 2b shows an XRD spectrum in the angular range of 10 ° to 25 ° 2 theta of the iron (III) orthophosphate from FIG. 2a.

Claims

Patent claims

1. A process for the preparation of iron (III) orthophosphate of the general formula FePO ₄ · nH ₂ O (n <2.5), in which a) an aqueous solution containing Fe ²⁺ ions is prepared by oxidizing an oxide (II) -, iron (III) - or mixed iron (II, III) compounds selected from hydroxides, oxides, oxide hydroxides, oxide hydrates, carbonates and hydroxide carbonates, together with elemental iron in an aqueous medium containing phosphoric acid and Fe Dissolving ²⁺ ions and reacting Fe ³⁺ with ele- mentary Fe (in a comproportionation reaction) to Fe ²⁺ , b) separating solids from the aqueous phosphoric Fe ²⁺ solution, c) to the aqueous phosphoric Fe ²⁺ An oxidizing agent is added to oxidize iron (II) in the solution, and iron (III) orthophosphate of the general formula FePO ₄ x nH ₂ O precipitates.

2. The method according to claim 1, characterized in that the phosphoric acid aqueous solution precipitating agents added to precipitate solids from the solution and separate from the phosphoric acid aqueous Fe ²⁺ solution, and / or that in the phosphoric acid aqueous solution dissolved metals electrolytic separates from the solution.

3. The method according to any one of the preceding claims, characterized in that the reaction of the oxidic iron compounds together with elemental iron in phosphoric acid-containing aqueous medium (stage a) at a temperature in the range of 15 ° C to 90 ⁰ C, preferably in the range of 20 ⁰ C to 75 ° C, more preferably in the range of 25 ° C to 65 ° C, and / or performs intensive mixing.

4. The method according to any one of the preceding claims, characterized in that the reaction of the oxidic iron compounds together with elemental iron in phosphoric acid-containing aqueous medium (stage a) for a period of 1 min to 120 min, preferably from 5 min to 60 min, more preferably from 20 minutes to 40 minutes.

5. The method according to any one of the preceding claims, characterized in that the concentration of phosphoric acid in the aqueous medium is 5% to 85%, preferably 10% to 40%, particularly preferably 15% to 30%, based on the weight of the aqueous solution ,

6. The method according to any one of the preceding claims, characterized in that the oxidizing agent which is added to oxidize iron (II) in the solution is an aqueous solution of hydrogen peroxide (H ₂ O ₂ ), preferably with a concentration of 15 to 50 wt .-%, particularly preferably 30 to 40 wt .-%.

7. The method according to any one of the preceding claims, characterized in that the oxidizing agent, which is added to oxidize iron (II) in the solution, is a selected under air, pure oxygen or ozone gaseous medium which is blown into the aqueous solution becomes.

8. The method according to any one of the preceding claims, characterized in that the iron (III) orthophosphate is separated after precipitation of the aqueous solution and preferably after separation at elevated temperature and / or dried under reduced pressure, or that the iron (lll ) orthophosphate after precipitation is provided as an aqueous dispersion having a solids content of 1 to 90% by weight.

9. iron (III) orthophosphate prepared according to any one of the preceding claims.

10. iron (III) orthophosphate, according to claim 9, characterized in that> 80 wt .-%, preferably> 90 wt .-%, particularly preferably> 95 wt .-% of iron (III) orthophosphats in the Metastrengit II (phosphosiderite) crystal structure.

11. iron (III) orthophosphate according to any one of claims 9 or 10, characterized in that it has at least in one dimension an average primary particle size <1 micron, preferably <500 nm, more preferably <300 nm, most preferably <100 nm.

12. iron (III) orthophosphate according to any one of claims 9 to 11, characterized in that it has a bulk density> 400 g / l, preferably> 700 g / l, more preferably> 1000 g / l and / or a tamped density> 600 g / l, preferably> 750 g / l, more preferably> 1100 g / l.

13. iron (III) orthophosphate according to one of claims 9 to 12, characterized in that it has a content of sodium and potassium of <300 ppm, preferably <200 ppm, more preferably <100 ppm and / or that it has a sulfur content of <300 ppm, preferably <200 ppm, particularly preferably <100 ppm, and / or that it has a nitrate content of <300 ppm, preferably <200 ppm, more preferably <100 ppm, and / or that it has a content of metals and transition metals, except iron, each <300 ppm, preferably <200 ppm, more preferably <100 ppm.

14. Use of iron (III) orthophosphate according to any one of the preceding claims for the production of LiFePCU cathode material for Li-ion batteries.

15. LiFePCU cathode material for Li-ion accumulators, prepared using iron (III) orthophosphate according to any one of the preceding claims.

16. A Li-ion secondary battery comprising a LiFePCU cathode material according to claim 15.